Canonical Allele Identifier: CA1123764
Gene: RPS27 HGNC NCBI

Linked Data

dbSNP Id: rs368279335
ExAC: 1:153963233 T / C
gnomAD v2: 1-153963233-T-C
gnomAD v3: 1-153990757-T-C
gnomAD v4: 1-153990757-T-C
MyVariant Identifiers: chr1:g.153963233T>C (hg19) chr1:g.153990757T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153990757T>C , CM000663.2:g.153990757T>C GRCh38
NC_000001.10:g.153963233T>C , CM000663.1:g.153963233T>C GRCh37
NC_000001.9:g.152229857T>C NCBI36
NG_053102.2:g.5003T>C

Transcript Alleles

HGVS Amino-acid Change
NM_001349946.1:c.-257T>C NP_001336875.1:n.-257T>C
NM_001349947.1:c.-368T>C NP_001336876.1:n.-368T>C
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